欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3414/001
药品名称Clensia
活性成分
    • CITRIC ACID ANHYDROUS 0.81 g
    • Macrogol 52.5 g
    • Potassium chloride 0.37 g
    • Simeticone 0.08 g
    • Sodium citrate 1.86 g
    • Sodium sulfate 3.75 g
    • Sodium chloride 0.73 g
剂型Powder for oral solution
上市许可持有人Alfasigma S.p.A. Viale Sarca, n. 223 20126 Milano (MI) Italië
参考成员国 - 产品名称Netherlands (NL)
Clensia poeder voor drank
互认成员国 - 产品名称
    • Germany (DE)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
    • Czechia (CZ)
      CLENSIA
    • Romania (RO)
      CLENSIA pulbere pentru soluţie orală
    • Slovakia (SK)
      Clensia
许可日期2016/06/22
最近更新日期2025/01/30
药物ATC编码
    • A06AD65 macrogol, combinations
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Fixed combination Art 10b Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
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